吡哆醇治疗三级卫生保健中心儿童早发特发性难治性癫痫的疗效研究

Jagadish N Bhadbhade
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Out of 64 patients Group A received 30 mg/kg/day pyridoxine with 4 mg/kg/day of oral prednisolone Group B received 4 mg/kg/day of oral prednisolone and 14, 15 randomly. The outcome of patients like episodes of seizure etc. was noted after 1 month of treatment. The statistical analysis was done by Chi-square test and analyzed by SPSS 19 version software. Result: In our study the average age in both the group was comparable with each other i.e. 3 ±1.21Yrs. and 3.52±1.31 Yrs. (p>0.05, t=1.12,df=62). The ratio of Male and Female was 2.9: 1 and 1.90: 1 was comparable with each other (X2=0.29, df=1,p>0.05). Complete seizure freedom was found in 34.38% and 9.38%; >50% seizure reduction but not complete cessation in 40.63% and 28.13%; <50% seizure reduction in 25.00% and 62.50% respectively in Group A and Group B which was statistically significant (X2=10.44, df=2,p<0.005). EEG findings Normal in 37.50% and 12.50%, Decreased Epileptiform discharges in 46.88% and 31.25%, Persistent Epileptiform discharges in 15.63% and 56.25% respectively in Group A and Group B this observed difference was statistically significant (X2=12.35, df=2,p<0.002) Conclusion: It can be concluded from our study that the patients who received the pyridoxine treatment improved much as compared to not received so the role of pyridoxine in the treatment of intractable seizure should not be underestimated. Key Word: Pyridoxine, Early-Onset Idiopathic Intractable Seizures, EEG Address for Correspondence: Dr. Jagadish N Bhadbhade, Assistant Professor, Department of Paediatrics, Vedaantaa Institute of Medical Sciences, At Saswand, Dhundalwadi, Talk. Dahanu, Dist. Palghar401602, Maharashtra, INDIA. Email: jagadish_bhadbhade@yahoo.co.in Received Date: 29/01/2019 Revised Date: 19/02/2019 Accepted Date: 14/03/2019 DOI: https://doi.org/10.26611/1014937 INTRODUCTION Pyridoxine is used for management of seizure disorder in three settings viz., seizures that respond to pyridoxine and require life-long supplementation with therapeutic doses of pyridoxine, pyridoxine dependent seizures (PDS, MIM 266100); early-onset seizures responsive to pyridoxine but not requiring life-long pyridoxine supplementation, pyridoxine-responsive seizures (PRS); and, high-dose pyridoxine for the treatment of major seizure disorders of young children e.g., West syndrome1. 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引用次数: 0

摘要

背景:吡哆醇用于治疗三种情况下的癫痫发作障碍,即:对吡哆醇有反应的癫痫发作,需要终生补充治疗剂量的吡哆醇,吡哆醇依赖性癫痫发作。目的和目的:研究吡哆醇在三级卫生保健中心儿科患者早发特发性难治性癫痫发作中的疗效。方法:本研究是一项横断面研究,在2017年6月至2018年6月的一年中,对64例儿童特发性难治性癫痫患者进行研究。患者的所有细节,如年龄、性别等都被记录下来。所有患者均行脑电图检查。64例患者中,A组给予吡哆醇30 mg/kg/d联合口服强的松龙4 mg/kg/d, B组给予口服强的松龙4 mg/kg/d,随机14、15例。治疗1个月后观察患者癫痫发作等情况。统计学分析采用卡方检验,统计学分析采用SPSS 19版软件。结果:两组患者的平均年龄具有可比性,均为3±1.21岁。(3.52±1.31)岁。(p > 0.05, t = 1.12, df = 62)。男女比例分别为2.9:1和1.90:1,具有可比性(X2=0.29, df=1,p>0.05)。完全发作自由分别为34.38%和9.38%;癫痫发作减少50%以上,但未完全戒烟的分别为40.63%和28.13%;A组和B组癫痫发作减少率分别为25.00%和62.50%,差异有统计学意义(X2=10.44, df=2,p<0.005)。A组和B组脑电图正常的分别为37.50%和12.50%,癫痫样放电减少的分别为46.88%和31.25%,持续癫痫样放电的分别为15.63%和56.25%,差异有统计学意义(X2=12.35, df=2,p<0.002)从我们的研究中可以得出结论,接受吡哆醇治疗的患者与未接受治疗的患者相比有很大的改善,因此吡哆醇在治疗顽固性癫痫发作中的作用不可低估。关键词:Pyridoxine,早发特发性顽固性癫痫,脑电图通讯地址:Jagadish N Bhadbhade博士,助理教授,Vedaantaa医学科学研究所儿科,At Saswand, Dhundalwadi, Talk。印度马哈拉施特拉邦帕尔加尔区达哈努401602电子邮件:jagadish_bhadbhade@yahoo.co.in接收日期:29/01/2019修订日期:19/02/2019接受日期:14/03/2019 DOI: https://doi.org/10.26611/1014937简介吡哆醇用于三种情况下的癫痫发作管理,即:对吡哆醇有反应的癫痫发作,需要终身补充治疗剂量的吡哆醇,吡哆醇依赖性癫痫发作(PDS, MIM 266100);早发性癫痫发作对吡哆醇有反应,但不需要终生补充吡哆醇,吡哆醇反应性癫痫发作(PRS);大剂量吡哆醇用于治疗幼儿的主要癫痫性疾病,如韦斯特综合征。有研究表明,吡哆醇依赖常常被误诊,这既因为偶尔的非典型表现2,也因为吡哆醇不经常使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A study efficacy of pyridoxine in early-onset idiopathic intractable seizures in pediatric patient at tertiary health care center
Background: Pyridoxine is used for management of seizure disorder in three settings viz., seizures that respond to pyridoxine and require life-long supplementation with therapeutic doses of pyridoxine, pyridoxine dependent seizures Aims and Objectives: study Efficacy of Pyridoxine in Early-Onset Idiopathic Intractable Seizures in pediatric patient at tertiary health care center. Methodology: This was a cross-sectional study carried out in the patients of Early-Onset Idiopathic Intractable Seizures in pediatric patient during the one year period i.e. June 2017 to June 2018, there were 64 pediatric patients with Idiopathic Intractable Seizures were enrolled for the study. All details of the patients like Age, sex etc. was noted. All the patients were undergone EEG testing. Out of 64 patients Group A received 30 mg/kg/day pyridoxine with 4 mg/kg/day of oral prednisolone Group B received 4 mg/kg/day of oral prednisolone and 14, 15 randomly. The outcome of patients like episodes of seizure etc. was noted after 1 month of treatment. The statistical analysis was done by Chi-square test and analyzed by SPSS 19 version software. Result: In our study the average age in both the group was comparable with each other i.e. 3 ±1.21Yrs. and 3.52±1.31 Yrs. (p>0.05, t=1.12,df=62). The ratio of Male and Female was 2.9: 1 and 1.90: 1 was comparable with each other (X2=0.29, df=1,p>0.05). Complete seizure freedom was found in 34.38% and 9.38%; >50% seizure reduction but not complete cessation in 40.63% and 28.13%; <50% seizure reduction in 25.00% and 62.50% respectively in Group A and Group B which was statistically significant (X2=10.44, df=2,p<0.005). EEG findings Normal in 37.50% and 12.50%, Decreased Epileptiform discharges in 46.88% and 31.25%, Persistent Epileptiform discharges in 15.63% and 56.25% respectively in Group A and Group B this observed difference was statistically significant (X2=12.35, df=2,p<0.002) Conclusion: It can be concluded from our study that the patients who received the pyridoxine treatment improved much as compared to not received so the role of pyridoxine in the treatment of intractable seizure should not be underestimated. Key Word: Pyridoxine, Early-Onset Idiopathic Intractable Seizures, EEG Address for Correspondence: Dr. Jagadish N Bhadbhade, Assistant Professor, Department of Paediatrics, Vedaantaa Institute of Medical Sciences, At Saswand, Dhundalwadi, Talk. Dahanu, Dist. Palghar401602, Maharashtra, INDIA. Email: jagadish_bhadbhade@yahoo.co.in Received Date: 29/01/2019 Revised Date: 19/02/2019 Accepted Date: 14/03/2019 DOI: https://doi.org/10.26611/1014937 INTRODUCTION Pyridoxine is used for management of seizure disorder in three settings viz., seizures that respond to pyridoxine and require life-long supplementation with therapeutic doses of pyridoxine, pyridoxine dependent seizures (PDS, MIM 266100); early-onset seizures responsive to pyridoxine but not requiring life-long pyridoxine supplementation, pyridoxine-responsive seizures (PRS); and, high-dose pyridoxine for the treatment of major seizure disorders of young children e.g., West syndrome1. It has been suggested that pyridoxine dependency is often underdiagnosed, both because of occasional atypical presentation2, and infrequent use of pyridoxine in Access this article online Quick Response Code: Website:
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